Clinical implications of neoadjuvant chemotherapy in advanced endometrial cancer: a multi-center retrospective cohort study

Background The mainstay of endometrial cancer treatment is surgical resection of tumors and postoperative adjuvant treatment is recommended if necessary. However, there is no consensus on the management of unresectable metastatic endometrial cancer. This study aimed to assess the feasibility and effectiveness of neoadjuvant chemotherapy followed by interval debulking surgery (NAC-IDS) in unresectable, metastatic endometrial cancer. Methods From the endometrial cancer cohorts of four institutions in Korea, we identified patients with International Federation of Gynecology and Obstetrics stages IIIC–IVB endometrial cancer who received NAC-IDS between January 2008 and December 2020. Through a medical record review, we collected patients’ clinicopathological data. Progression-free survival (PFS), overall survival (OS), and the factors affecting survival outcomes were analyzed. Results Overall, 32 patients were included with endometrioid (n = 18), serous (n = 5), carcinosarcoma (n = 6), and other histological types (n = 3). Among them, 28 (87.5%) patients had stage IVB disease. The most common neoadjuvant chemotherapy (NAC) regimen was paclitaxel-carboplatin (n = 25, 78.1%), which was administered for a median of six cycles. While 26 (81.3%) patients showed an objective response, two (6.3%) progressed despite NAC. At the time of interval debulking surgery (IDS), 23 (71.9%) patients achieved complete cytoreduction. During 31.0 months of the median follow-up, there were 23 recurrences and 11 deaths, corresponding to a median PFS of 19.7 months and a 3-year OS rate of 69.7%. In multivariate analyses, non-endometrioid histology and residual tumor after IDS were identified as independent poor prognostic factors for PFS (adjusted hazard ratio [HR], 7.322; P < 0.001 and 5.934; P = 0.001, respectively). Multivariate analysis for OS could not be conducted because of the small number of events, although non-endometrioid histology was the only factor associated with worse OS in univariate analysis (adjusted HR, 4.523; P = 0.032). Conclusions NAC-IDS may be a treatment option for unresectable metastatic endometrial cancer. Tumor histology and the possibility of complete cytoreduction are the primary considerations for NAC-IDS. Supplementary Information The online version contains supplementary material available at 10.1186/s12885-022-09746-3.

cancer in developed countries. The incidence of EC has gradually increased in Korea [2]. Most patients with EC are diagnosed at an early stage and have an excellent 5-year survival rate (94.9%). In contrast, patients with EC diagnosed at an advanced stage show poor prognosis, with 17.8% of them having a 5-year survival rate [3][4][5][6]. The mainstay of EC management is the surgical resection of tumors. Postoperative adjuvant treatment is recommended for patients with high-risk pathological factors.
In the literature, the residual tumor size after cytoreductive surgery has been reported as one of the most reliable prognostic factors in advanced EC, similar to epithelial ovarian cancer. Chi et al. investigated the survival impact of surgical cytoreduction in 55 patients with stage IV EC and found that the optimal cytoreduction group had significantly better overall survival (OS) than the suboptimal or unresectable groups [7]. Similarly, Memarzadeh et al. assessed 43 patients with stages III-IV papillary serous EC who underwent primary debulking surgery (PDS) and found that patients with microscopic residual disease had significantly improved progressionfree survival (PFS) and OS compared to those with macroscopic residual disease after surgery [8].
To date, there is no consensus on the management of unresectable metastatic EC [9,10]. In particular, uterine serous carcinoma, a highly aggressive histologic subtype accounting for 10% of all EC cases, has clinical features similar to those of ovarian serous carcinoma: a high tendency of intra-abdominal metastasis at diagnosis and poor prognosis with a high recurrence rate [11,12]. Accordingly, a few studies have been conducted to determine whether neoadjuvant chemotherapy (NAC) followed by interval debulking surgery (IDS) is also applicable to unresectable metastatic uterine serous carcinoma. Bogani et al. investigated 30 patients with stage IVB uterine serous carcinoma between 2005 and 2016. Compared to patients who underwent PDS (n = 15), those who underwent neoadjuvant chemotherapy followed by interval debulking surgery (NAC-IDS) (n = 15) showed similar PFS and OS, a shorter length of hospital stay and operative time, and lower perioperative transfusion rate [13]. Furthermore, De Lange et al. investigated 102 patients with International Federation of Gynecology and Obstetrics (FIGO) stages III-IV EC who underwent NAC-IDS and reported similar response rates to NAC for endometrioid and serous tumors [14].
Based on previous studies, the use of NAC might increase the probability of achieving optimal debulking and improve survival outcomes in advanced EC, while decreasing the extent of surgery and surgery-related complications. However, only a few studies have investigated whether NAC could be a possible option for unresectable metastatic EC encompassing all histological subtypes. Therefore, we aimed to assess the feasibility and effectiveness of NAC-IDS in unresectable metastatic EC, including the serous histologic type and others. We also investigated prognostic factors associated with survival outcomes after NAC-IDS.

Study population
We identified patients with FIGO stages IIIC-IVB disease who underwent NAC-IDS for metastatic EC between January 2008 and December 2020, from the EC cohorts of four institutions in Korea: Seoul National University Hospital, Seoul National University Bundang Hospital, Seoul Metropolitan Government Seoul National University Boramae Medical Center and National Cancer Center. Among them, we excluded patients with the following conditions: (1) those with uterine sarcoma, e.g., leiomyosarcoma, endometrial stromal sarcoma, and undifferentiated sarcoma; (2) those who had been diagnosed with other malignancies before the diagnosis of EC; and (3) those who had insufficient clinicopathologic data.

Data collection
The following information was collected from patients' medical records: age at diagnosis, menopausal status, body mass index, FIGO stage, histologic subtype and grade, serum cancer antigen (CA)-125 levels, NAC regimens, and number of NAC cycles. The extent of interval debulking surgery (IDS) and residual tumor after surgery and postoperative adjuvant treatments were also collected. Baseline imaging studies, such as computed tomography (CT), magnetic resonance imaging, and 18 F-fluorodeoxyglucose positron emission tomography/ CT scans, were reviewed, and the locations of metastatic disease at diagnosis were investigated.
Patients underwent routine CT every two or three cycles of chemotherapy and every 3 months for the first 2 years, every 4-6 months for the next 2 years, and every year thereafter. Response to NAC and disease progression were evaluated based on imaging studies, as per the Response Evaluation Criteria in Solid Tumors version 1.1 [15]. In terms of survival data, we defined PFS and OS as the interval from initial diagnosis to disease progression (recurrence) and cancer-related death or the last followup, respectively.

Statistical analysis
We analyzed the baseline characteristics and survival outcomes of the study population using descriptive analysis. To investigate prognostic factors associated with survival outcomes after NAC-IDS, we divided the study population into two groups according to the size of the residual tumor after IDS (no gross residual tumor [NGR] versus [vs.] any residual tumor) and histological subtype (endometrioid vs. non-endometrioid). Then, we compared clinicopathological characteristics between the two groups using the Student t-or Mann-Whitney U test for continuous variables and the Pearson chi-square or Fisher exact test for categorical variables. The Kaplan-Meier method was used to estimate survival curves. Differences in survival between the two groups were tested using the log-rank test. In multivariate analysis, we adjusted variables that were significant in univariate analyses. Cox proportional hazards regression analyses were conducted to calculate hazard ratios (HRs) and 95% confidence intervals (CIs).
All statistical analyses were performed using SPSS statistical software (version 25.0; IBM Corp., Armonk, NY, USA). Statistical significance was set at P < 0.05, based on a two-sided hypothesis.

All study patients
In total, 32 patients were included in the analysis. Table 1 presents the clinicopathological characteristics of the patients. The median patient age and serum CA-125 level at initial diagnosis were 56 years and 192.7 IU/mL, respectively. Most patients (28/32, 87.5%) had FIGO stage IVB disease, and the most common histologic subtype was endometrioid adenocarcinoma (n = 18, 56.3%), followed by carcinosarcoma (n = 6, 18.8%) and serous adenocarcinoma (n = 5, 15.6%). The other three patients had clear cell carcinoma, small cell neuroendocrine carcinoma, and mesonephric adenocarcinoma, respectively. The grading information of patients with endometrioid histologic subtypes was presented as follows: grade 1 and 2 disease as 'low grade' , while grade 3 disease as 'high grade. ' Table 2 displays the initial locations of metastatic disease observed in the baseline imaging studies. Most common distant metastatic sites were lung/pleural seeding and distant lymph node such as supraclavicular lymph node, internal mammary lymph node, etc.

Comparisons by residual tumor and histologic subtype
Next, we compared the clinicopathological characteristics and survival outcomes between patients who achieved complete cytoreduction (no gross residual [NGR], n = 23) and those who did not (n = 9). As shown in Table 3, similar baseline characteristics were observed between the two groups; however, the objective response rate was significantly higher in the NGR group than in the any residual tumor group (95.7% vs. 44.4%; P = 0.008). In addition, the NGR group showed better PFS (median, 24.6 vs. 13.7 months; P = 0.041) but similar OS (P = 0.111) (Fig. 2 A, B).
We also compared the clinicopathologic characteristics and survival outcomes between patients with the endometrioid histologic subtype (n = 18) and those with the non-endometrioid histologic subtype (n = 14). The endometrioid and non-endometrioid groups showed similar baseline characteristics even in response to NAC, except for tumor grade (Table 4). In survival analyses, the endometrioid group showed significantly better PFS (median, 33.2 vs. 12.7 months; P = 0.003) and 3-year OS rates ; P = 0.020) than the non-endometrioid group (Fig. 2 C, D). In the endometrioid group, patients who achieved complete cytoreduction (n = 12) and those who did not (n = 6) showed similar PFS (P = 0.051) and OS (P = 0.078) in spite of their tendency of better survival than those with residual tumor after surgery. However, in the nonendometrioid group, patients who achieved complete cytoreduction (n = 11) had significantly better PFS (median, 18.9 vs. 5.5 months; P = 0.005) and OS (3-year OS rate, 47.7% vs. 33.3%; P = 0.046) than those with any residual tumor (n = 3) (Supplementary Fig. 1 A-D).

Discussion
In this multicenter study, approximately 80% of patients showed an objective response to NAC, and 70% achieved complete cytoreduction with no gross residual. The median PFS of all patients was 19.7 months, while the 3-year OS rate was 69.7%, suggesting that NAC-IDS may be a feasible treatment option in this study population. Complete resection of metastatic tumors during surgery is a well-known prognostic factor in advanced-stage EC, similar to advanced-stage epithelial ovarian cancer [7,8,16]. Moreover, in cases of unresectable metastatic EC, upfront surgery may be futile but may increase perioperative complications and morbidities. In advancedstage epithelial ovarian cancer, many studies have reported that NAC-IDS is associated with similar survival outcomes and lower perioperative complications and morbidities than upfront surgery or PDS. For example, in a phase III CHORUS trial, Kehoe et al. revealed that OS with NAC-IDS was non-inferior to PDS in patients with stages III-IV ovarian cancer (median, 24.1 months vs. 22.6 months; HR, 0.87; 95% CI, 0.72-1.05) [17]. In another phase III randomized controlled trial (RCT), Vergote et al. concluded that NAC-IDS was not inferior to PDS as a treatment option for patients with stages IIIC-IV ovarian cancer [18]. However, to date, no RCT has compared the efficacy of NAC-IDS and PDS as a primary treatment strategy for endometrial cancer. Nevertheless, gynecologic oncologists have used NAC-IDS for the management of EC, including serous and other histological subtypes. Previously, De Lange et al. reported that the response rate to NAC was similar between EC patients with endometrioid and serous histologic subtypes [14]. According to a large cohort study from the National Cancer Database, the diagnosis of EC more recently, stage IVB disease, and serous histology were associated with an increased rate of NAC. Moreover, patients with NAC-IDS had a decreased risk of early death, including postoperative mortality, but had a worse long-term prognosis [4]. Furthermore, Khouri et al. suggested the importance of response to NAC and the execution of IDS. In that study, patients who responded to NAC and received IDS showed significantly better OS than those who received NAC but not IDS owing to disease progression (median 16 vs. 6 months, P = 0.037) [19].
In the current study, two patients showed disease progression despite NAC. One patient (stage IVB carcinosarcoma, case 4 in Supplementary Table 1) received four cycles of paclitaxel plus carboplatin combination chemotherapy as NAC, and the residual tumor size after IDS was larger than 2 cm. The other patient (stage IVB endometrioid adenocarcinoma, case 14 in Supplementary Table 1) received two cycles of paclitaxel-carboplatin combination chemotherapy and palliative surgery, including low anterior resection and small bowel resection due to tumoro-enteral fistula. Only one cycle of postoperative adjuvant chemotherapy was administered to both patients owing to their poor general condition. The patients died 11.1 and 5.9 months after initial diagnosis, respectively.
Compared with previous studies, our study has several unique features. First, while previous studies included patients who received NAC for 3-6 cycles, 34.4% (11/32) of our study population received > 6 cycles of NAC. Although all 11 patients received NAC as palliative chemotherapy for salvage intent, not curative intent, all of them achieved complete cytoreduction after a number of cycles of NAC. This might be the reason why PFS in this study population appears to be at the upper end of the range described in previous studies: 12-18 months in the NAC groups [11][12][13][14]19]. Second, various firstline chemotherapy regimens were used in the current study. Third, two patients in our study population had  been misdiagnosed with node-positive cervical cancer; therefore, they initially received paclitaxel-cisplatinbevacizumab, followed by radical hysterectomy and lymphadenectomy. After surgery, the final diagnosis was corrected to endometrioid EC based on the pathological findings. Nevertheless, we believe that such unique features reflect real-world practice of unresectable metastatic EC.
Regarding factors affecting survival outcomes after NAC-IDS, we found that the non-endometrioid histologic subtype and any residual tumor after IDS were independent poor prognostic factors for PFS, which is consistent with previous studies' findings [11,12,20]. Of two, non-endometrioid histologic subtype was associated with worse OS in univariate analysis, but we could not conduct further multivariate analysis due to the small sample size.
Recent advances in molecular classification and the development of novel therapeutic agents have opened a new avenue for the treatment of recurrent metastatic EC. According to the KEYNOTE-158 trial, for microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) recurrent tumors, monotherapy with pembrolizumab, an immune checkpoint inhibitor targeting programmed cell death protein 1, showed an objective response rate of 57.1%, which is a very encouraging outcome in recurrent settings [21]. In the phase III KEYNOTE-775 trial, even for patients with tumors that were not MSI-H or dMMR, the combination of pembrolizumab and lenvatinib demonstrated significantly better PFS and OS than treatment of physician's choice [22]. Based on the results of these trials, conducting molecular immunohistochemistry (IHC) for mismatch repair (MMR) proteins is increasing nowadays. However, there were only 15 patients whose tissue were tested for dMMR and only three patients had dMMR tumors in this population. More information on IHC including MMR proteins (MLH1, MSH2, MSH6, and PMS2) and p53 were shown in Supplementary Table 1. Currently, two phase III RCTs are ongoing for newly diagnosed advanced or recurrent EC: the ENGOT-en9/LEAP-001 trial, comparing the efficacy and safety of pembrolizumab plus lenvatinib combination therapy vs. paclitaxel-carboplatin [23], and the ENGOT-en6/NSGO-RUBY trial, comparing the efficacy and safety of dostarlimab plus paclitaxelcarboplatin vs. placebo plus paclitaxel-carboplatin [24]. If these two trials commonly result in positive results from the experimental arms, incorporation of immune checkpoint inhibitors might further expand the use of NAC in the management of unresectable metastatic EC.
Our study has several limitations. First, because of the retrospective study design, there might be inevitable issues such as selection bias. Second, although we collected relevant patients from four institutions over the past 13 years, owing to the rarity of unresectable metastatic EC cases with NAC-IDS, the sample size was small, making it difficult to conduct reliable multivariate and subgroup analyses. Third, there may have been heterogeneity among physicians and centers. Finally, NAC-related adverse events, perioperative complications, and quality of life issues were not investigated.

Conclusions
The current study's results demonstrate that NAC-IDS may be a treatment option for unresectable metastatic EC. For selection of appropriate candidates for the NAC-IDS strategy, the tumor histology and possibility of complete cytoreduction should be the primary considerations. Further large-scale, prospective cohort studies are required.